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Perioperative respiratory complications following awake and deeply laryngeal mask airways removal in children: a prospective multicentre randomized controlled trial

Perioperative respiratory complications following awake and deeply laryngeal mask airways removal in children: a prospective multicentre randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015233
Enrollment
Unknown
Registered
2018-03-16
Start date
2018-04-01
Completion date
Unknown
Last updated
2018-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative respiratory complications following laryngeal mask airways removal in children

Interventions

Awake Group:Awake removal of the laryngeal mask airway, be awake as defined by children who is able to open eyes, cry, move body, active facial muscle after stimulating.
Deep Group:LMA removed whilst deeply anaesthetised, be deeply anaesthetized as defined by CETSev was maintained at 1.8%, the spontaneous breathing was to be restored (VT = 4 ml/kg, PETCO2 in 35 ~ 45 m

Sponsors

Zhongshan Ophthalmic Center of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: Children undergoing ophthalmic or urological surgery with LMA, aged 3 ~ 6, ASA physical status I~II, any gender, anesthesia duration at least 30 minutes

Exclusion criteria

Exclusion criteria: 1) with acute upper respiratory infection; 2) in the acute stage of asthma or acute bronchitis; 3) with allergic rhinitis, allergic dermatitis and other allergic diseases; 4) having the risk of false aspiration; 5) predictably difficult airway; 6) abnormal facial anatomy; 7) hearing impairment; 8) congenital heart disease or nervous system disease; 9) sleep apnea syndrome; 10) gastroesophageal reflux; 11) the children who failed to be inserted in the laryngeal mask for three times and need the tracheal intubation.

Design outcomes

Primary

MeasureTime frame
Perioperative respiratory adverse events;

Secondary

MeasureTime frame
PACU stay time after surgery;Emergence agitation;Awake time;Spontaneous breathing recovery time;Laryngeal mask removal timing;

Countries

China

Contacts

Public ContactXiaoliang Gan

Zhongshan Ophthalmic Center, Sun Yat-sun University

ganxiaoliang@yeah.net+86 13688893908

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026